Dipeptidyl peptidase IV inhibitors as novel regulators of vascular disease

被引:14
作者
Akoumianakis, Ioannis [1 ]
Antoniades, Charalambos [1 ]
机构
[1] Univ Oxford, Div Cardiovasc Med, Oxford, England
关键词
Atherosclerosis; Oxidative stress; Perivascular adipose tissue; DPP-IV inhibitors; GLP-1 RECEPTOR AGONISTS; CARDIOVASCULAR OUTCOMES; OXIDATIVE STRESS; DPP-4; INHIBITOR; ADIPOSE-TISSUE; INFLAMMATION; SITAGLIPTIN; OBESITY; HEART; LIRAGLUTIDE;
D O I
10.1016/j.vph.2017.07.001
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Dipeptidyl peptidase IV (DPP-IV) has been revealed as an adipokine with potential relevance in cardiovascular disease (CVD), while clinically used DPP-IV inhibitors have demonstrated beneficial cardiovascular effects in several experimental studies. Perivascular adipose tissue (PVAT) is a unique adipose tissue depot in close anatomical proximity and bidirectional functional interaction with the vascular wall, which is a source of DPP-IV and its biology may be influenced by DPP-IV inhibition. Recently, DPP-IV inhibition has been associated with decreased local inflammation and oxidative stress both in the vascular wall and the PVAT, potentially regulating atherogenesis progression in vivo. DPP-IV inhibition may thus be a promising target in cardiovascular disease. However, the exact pleiotropic mechanisms that underlie the cardiovascular effects of DPP-IV inhibition need to be clarified, while the in vivo benefit of DPP-IV inhibition in humans remains unclear.
引用
收藏
页码:1 / 4
页数:4
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